Canonical Allele Identifier: PA2827766669
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 3067140
ClinVar RCV Id: RCV003992829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Phe1404Ile
CA349049950
NM_001353950.2:c.4210T>A